Senior Statistical Programmer I/ii (cvrm)

AstraZeneca

Warsaw, Poland
3d onsite
Excellent programming skills in sas
Knowledge of clinical development process
Ability to manage relevant documentation
Join a fast-paced and agile global team at AstraZeneca CVRM

Job Summary

  • Join a fast-paced and agile global team at AstraZeneca CVRM.
  • You will lead programming deliverables for clinical studies with a focus on quality and timeliness.
  • This role offers opportunities for innovation and continuous improvement in drug development.

Matching Summary

Join a fast-paced and agile global team at AstraZeneca CVRM.

Skills & Requirements

Must-have

  • Excellent programming skills in SAS
  • Knowledge of clinical development process
  • Ability to manage relevant documentation

Nice-to-have

  • Experience in regulatory submissions
  • Broad experience across therapeutic areas
  • Ability to influence stakeholders

Key Requirements

  • Degree in Mathematics, Statistics, or related field
  • Proficient in SAS or R programming
  • Current knowledge of regulatory requirements

Work Rights

Not specified

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